Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11167764 0.925 0.120 5 142099500 regulatory region variant A/C snv 0.80 2
rs199883290 0.925 0.120 16 50729867 missense variant G/A;C snv 4.0E-06; 1.5E-02 7.0E-06 2
rs224136 0.925 0.120 10 62710915 intron variant C/A;T snv 0.34 2
rs540973741 0.925 0.120 16 50729868 frameshift variant C/-;CC delins 2
rs8005161 0.882 0.120 14 88006251 intron variant C/T snv 0.18 3
rs11175593 0.882 0.160 12 40208138 non coding transcript exon variant C/T snv 2.8E-02 3
rs11190140 0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55 4
rs1456893 0.851 0.160 7 50230076 intron variant G/A snv 0.69 3
rs1551398 0.882 0.160 8 125527809 intron variant G/A snv 0.48 3
rs1736135 0.851 0.160 21 15432901 intron variant T/C snv 0.33 4
rs17582416 0.882 0.160 10 34998722 regulatory region variant T/G snv 0.31 3
rs2188962 0.882 0.160 5 132435113 intron variant C/T snv 0.29 4
rs3828309 0.882 0.160 2 233271764 intron variant A/G snv 0.42 3
rs4263839 0.807 0.160 9 114804160 intron variant A/G snv 0.75 3
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 3
rs11584383 0.827 0.200 1 200966738 downstream gene variant T/C snv 0.24 4
rs13003464 0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs1847472 0.807 0.200 6 90263440 intron variant C/A snv 0.25 3
rs2274910 0.827 0.200 1 160882256 non coding transcript exon variant T/C snv 0.65 0.58 3
rs5743293 0.807 0.200 16 50729868 frameshift variant C/-;CC delins 2
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 4
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 3
rs11747270 0.790 0.240 5 150879305 intron variant A/G snv 0.21 3
rs4613763 0.851 0.240 5 40392626 regulatory region variant T/C snv 0.14 3
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5